01 2Apitoria Pharma Private Limited Unit-II
02 1Astellas Ireland Co. Limited
03 1Astellas Pharma Inc. Takahagi Technology Center
04 3Aurobindo Pharma Limited (Unit-VIII)
05 1Boryung Pharmaceutical Co., Ltd.
06 2Curia Spain SAU
07 1Divi's Laboratories Limited
08 1Dongbang FTL Co., Ltd.
09 1Hanseochem Co., Ltd.
10 1Lee Pharma Limited
11 2Lee Pharma Limited@Lee Pharma Limited
12 1Suven Pharmaceutical Limited
13 2Suven Pharmaceuticals Limited
14 1Swati Spentose Private Limited (Unit-I)
15 2Synthon, sro
16 1Zhejiang Jinhua Conba Bio-Pharm Co., Ltd
A Tamsulosin Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tamsulosin Hydrochloride, including repackagers and relabelers. The FDA regulates Tamsulosin Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tamsulosin Hydrochloride API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Tamsulosin Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tamsulosin Hydrochloride supplier is an individual or a company that provides Tamsulosin Hydrochloride active pharmaceutical ingredient (API) or Tamsulosin Hydrochloride finished formulations upon request. The Tamsulosin Hydrochloride suppliers may include Tamsulosin Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Tamsulosin Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Tamsulosin Hydrochloride Drug Master File in Korea (Tamsulosin Hydrochloride KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Tamsulosin Hydrochloride. The MFDS reviews the Tamsulosin Hydrochloride KDMF as part of the drug registration process and uses the information provided in the Tamsulosin Hydrochloride KDMF to evaluate the safety and efficacy of the drug.
After submitting a Tamsulosin Hydrochloride KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Tamsulosin Hydrochloride API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Tamsulosin Hydrochloride suppliers with KDMF on PharmaCompass.
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